A citation-based method for searching scientific literature

Jean Xavier, Bo Zhou, Frédéric Bilan, Xianglong Zhang, Brigitte Gilbert-Dussardier, Sylvie Viaux-Savelon, Reenal Pattni, Steve S Ho, David Cohen, Douglas F Levinson, Alexander E Urban, Claudine Laurent-Levinson. NPJ Genom Med 2018
Times Cited: 4







List of co-cited articles
9 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


1q21.1 Microduplication expression in adults.
Alessia Dolcetti, Candice K Silversides, Christian R Marshall, Anath C Lionel, Dimitri J Stavropoulos, Stephen W Scherer, Anne S Bassett. Genet Med 2013
58
75

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
Nicola Brunetti-Pierri, Jonathan S Berg, Fernando Scaglia, John Belmont, Carlos A Bacino, Trilochan Sahoo, Seema R Lalani, Brett Graham, Brendan Lee, Marwan Shinawi,[...]. Nat Genet 2008
389
50

Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series.
Martina Busè, Helenia C Cuttaia, Daniela Palazzo, Marcella V Mazara, Salvatrice A Lauricella, Michela Malacarne, Mauro Pierluigi, Simona Cavani, Maria Piccione. Ital J Pediatr 2017
15
50

Narrowing the Genetic Causes of Language Dysfunction in the 1q21.1 Microduplication Syndrome.
Antonio Benítez-Burraco, Montserrat Barcos-Martínez, Isabel Espejo-Portero, Maite Fernández-Urquiza, Raúl Torres-Ruiz, Sandra Rodríguez-Perales, Ma Salud Jiménez-Romero. Front Pediatr 2018
5
50

Phenotypic Variability Associated with a Large Recurrent 1q21.1 Microduplication in a Three-Generation Family.
Judith M A Verhagen, Nicole de Leeuw, Dimitri N M Papatsonis, Els W M Grijseels, Ronald R de Krijger, Marja W Wessels. Mol Syndromol 2015
11
50

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
Heather C Mefford, Andrew J Sharp, Carl Baker, Andy Itsara, Zhaoshi Jiang, Karen Buysse, Shuwen Huang, Viv K Maloney, John A Crolla, Diana Baralle,[...]. N Engl J Med 2008
514
50

Understanding the impact of 1q21.1 copy number variant.
Chansonette Harvard, Emma Strong, Eloi Mercier, Rita Colnaghi, Diana Alcantara, Eva Chow, Sally Martell, Christine Tyson, Monica Hrynchak, Barbara McGillivray,[...]. Orphanet J Rare Dis 2011
39
50

Connexin 50 gene on human chromosome 1q21 is associated with schizophrenia in matched case control and family-based studies.
Xingqun Ni, Jose Valente, Maria H Azevedo, Michelle T Pato, Carlos N Pato, James L Kennedy. J Med Genet 2007
22
50

Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder.
Olafur O Gudmundsson, G Bragi Walters, Andres Ingason, Stefan Johansson, Tetyana Zayats, Lavinia Athanasiu, Ida Elken Sonderby, Omar Gustafsson, Muhammad S Nawaz, Gudbjorn F Jonsson,[...]. Transl Psychiatry 2019
20
50

Chromosomal microarray analysis and prenatal diagnosis.
Jamie O Lo, Brian L Shaffer, Cori D Feist, Aaron B Caughey. Obstet Gynecol Surv 2014
14
25

Clinical and molecular cytogenetic analyses of four families with 1q21.1 microdeletion or microduplication.
Hong-Dan Wang, Lin Liu, Dong Wu, Tao Li, Cun-Ying Cui, Lian-Zhong Zhang, Cheng-Zeng Wang. J Gene Med 2017
9
25

Prenatal diagnosis of an atypical 1q21.1 microdeletion and duplication associated with foetal urogenital abnormalities.
Can Liao, Fang Fu, Cui-Xing Yi, Ru Li, Xin Yang, Qin Xu, Dong-Zhi Li. Gene 2012
6
25

Application of array-comparative genomic hybridization in tetralogy of Fallot.
Lin Liu, Hong-Dan Wang, Cun-Ying Cui, Dong Wu, Tao Li, Tai-Bing Fan, Bang-Tian Peng, Lian-Zhong Zhang, Cheng-Zeng Wang. Medicine (Baltimore) 2016
5
25

A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot.
Valentina Guida, Rosangela Ferese, Marcella Rocchetti, Monica Bonetti, Anna Sarkozy, Serena Cecchetti, Vania Gelmetti, Francesca Lepri, Massimiliano Copetti, Giuseppe Lamorte,[...]. Eur J Hum Genet 2013
24
25

Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways.
Candice K Silversides, Anath C Lionel, Gregory Costain, Daniele Merico, Ohsuke Migita, Ben Liu, Tracy Yuen, Jessica Rickaby, Bhooma Thiruvahindrapuram, Christian R Marshall,[...]. PLoS Genet 2012
106
25

1q21.1 Duplication syndrome and epilepsy: Case report and review.
Ioulia Gourari, Romaine Schubert, Aparna Prasad. Neurol Genet 2018
5
25


Phenotypic variability and genetic susceptibility to genomic disorders.
Santhosh Girirajan, Evan E Eichler. Hum Mol Genet 2010
185
25

Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
89
25

Regulation of human heart contractility by essential myosin light chain isoforms.
M Morano, U Zacharzowski, M Maier, P E Lange, V Alexi-Meskishvili, H Haase, I Morano. J Clin Invest 1996
97
25

New microdeletion and microduplication syndromes: A comprehensive review.
Julián Nevado, Rafaella Mergener, María Palomares-Bralo, Karen Regina Souza, Elena Vallespín, Rocío Mena, Víctor Martínez-Glez, María Ángeles Mori, Fernando Santos, Sixto García-Miñaur,[...]. Genet Mol Biol 2014
54
25


Complex genetics of radial ray deficiencies: screening of a cohort of 54 patients.
Sarah Vergult, A Jeannette M Hoogeboom, Emilia K Bijlsma, Tom Sante, Eva Klopocki, Bram De Wilde, Marjolijn Jongmans, Christian Thiel, Joke B G M Verheij, Antonio Perez-Aytes,[...]. Genet Med 2013
9
25

An estimation of the prevalence of genomic disorders using chromosomal microarray data.
Madelyn A Gillentine, Philip J Lupo, Pawel Stankiewicz, Christian P Schaaf. J Hum Genet 2018
15
25

A de novo mosaic mutation in SPAST with two novel alternative alleles and chromosomal copy number variant in a boy with spastic paraplegia and autism spectrum disorder.
A M Matthews, M Tarailo-Graovac, E M Price, I Blydt-Hansen, A Ghani, B I Drögemöller, W P Robinson, C J Ross, W W Wasserman, H Siden,[...]. Eur J Med Genet 2017
8
25

Prenatal Diagnosis of Recurrent Distal 1q21.1 Duplication in Three Fetuses With Ultrasound Anomalies.
Xiuqing Ji, Qiong Pan, Yan Wang, Yun Wu, Jing Zhou, An Liu, Fengchang Qiao, Dingyuan Ma, Ping Hu, Zhengfeng Xu. Front Genet 2018
2
50

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls.
Rachel Soemedi, Ana Topf, Ian J Wilson, Rebecca Darlay, Thahira Rahman, Elise Glen, Darroch Hall, Ni Huang, Jamie Bentham, Shoumo Bhattacharya,[...]. Hum Mol Genet 2012
72
25

Clinical aspects of prenatally detected congenital heart malformations and the yield of chromosomal microarray analysis.
Rivka Sukenik-Halevy, Shay Sukenik, Arie Koifman, Yoav Alpert, Reli Hershkovitz, Alex Levi, Tal Biron-Shental. Prenat Diagn 2016
11
25

Congenital Heart Disease: Prenatal Diagnosis and Genetic Associations.
Maeve K Hopkins, Lorraine Dugoff, Jeffrey A Kuller. Obstet Gynecol Surv 2019
1
100

Chromosomal Aberrations in Pediatric Patients with Developmental Delay/Intellectual Disability: A Single-Center Clinical Investigation.
Ting Hu, Zhu Zhang, Jiamin Wang, Qinqin Li, Hongmei Zhu, Yi Lai, He Wang, Shanling Liu. Biomed Res Int 2019
5
25

Cardiovascular malformations among preterm infants.
Kirsty Tanner, Nilofer Sabrine, Christopher Wren. Pediatrics 2005
142
25

Attitudes Towards Prenatal Genetic Counseling, Prenatal Genetic Testing, and Termination of Pregnancy among Southeast and East Asian Women in the United States.
Ginger J Tsai, Carrie A Cameron, Jennifer L Czerwinski, Hector Mendez-Figueroa, Susan K Peterson, Sarah Jane Noblin. J Genet Couns 2017
9
25

Chromosome 15q13 microduplication in a fetus with cardiac rhabdomyoma: a case report.
Chen-Zhao Lin, Bi-Ru Qi, Jian-Su Hu, Yu-Dian Huang, Xiu-Qiong Huang. Mol Cytogenet 2019
3
33


A fetus with Kabuki syndrome 2 detected by chromosomal microarray analysis.
Chen-Zhao Lin, Bi-Ru Qi, Jian-Su Hu, Xiu-Qiong Huang. Int J Clin Exp Pathol 2020
4
25

Chromosomal uniparental disomy 16 and fetal intrauterine growth restriction.
Xie Yingjun, Hu Zhiyang, Lin Linhua, Su Fangming, Huang Linhuan, Tan Jinfeng, Pang Qianying, Sun Xiaofang. Eur J Obstet Gynecol Reprod Biol 2017
9
25

Changing Landscape of Congenital Heart Disease.
Berto J Bouma, Barbara J M Mulder. Circ Res 2017
65
25

Detection of copy number variants using chromosomal microarray analysis for the prenatal diagnosis of congenital heart defects with normal karyotype.
Tingting Song, Shanning Wan, Yu Li, Ying Xu, Yinghui Dang, Yunyun Zheng, Chunyan Li, Jiao Zheng, Biliang Chen, Jianfang Zhang. J Clin Lab Anal 2019
7
25

Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies.
Elizabeth Goldmuntz, Prasuna Paluru, Joseph Glessner, Hakon Hakonarson, Jaclyn A Biegel, Peter S White, Xiaowu Gai, Tamim H Shaikh. Congenit Heart Dis 2011
52
25


Congenital heart disease: a global public health concern.
Joseph W Rossano. Lancet Child Adolesc Health 2020
5
25

Cardiovascular anomalies in Turner syndrome: spectrum, prevalence, and cardiac MRI findings in a pediatric and young adult population.
Hee Kyung Kim, William Gottliebson, Kan Hor, Philippe Backeljauw, Iris Gutmark-Little, Shelia R Salisbury, Judy M Racadio, Kathy Helton-Skally, Robert Fleck. AJR Am J Roentgenol 2011
72
25

Chromosome 16p13.11 Microdeletion Syndrome in a Newborn: A Case Study.
Amanda Elizabeth Smith, Amy Jnah, Desi Newberry. Neonatal Netw 2018
3
33

Prenatal diagnosis of congenital heart disease: A review of current knowledge.
Nathalie Jeanne Bravo-Valenzuela, Alberto Borges Peixoto, Edward Araujo Júnior. Indian Heart J 2018
18
25

Global birth prevalence of congenital heart defects 1970-2017: updated systematic review and meta-analysis of 260 studies.
Yingjuan Liu, Sen Chen, Liesl Zühlke, Graeme C Black, Mun-Kit Choy, Ningxiu Li, Bernard D Keavney. Int J Epidemiol 2019
129
25

1q21.1 microduplication in a patient with mental impairment and congenital heart defect.
Guowen Sun, Zhiping Tan, Liangliang Fan, Jian Wang, Yifeng Yang, Weizhi Zhang. Mol Med Rep 2015
6
25


Congenital heart disease and genetic syndromes: new insights into molecular mechanisms.
Giulio Calcagni, Marta Unolt, Maria Cristina Digilio, Anwar Baban, Paolo Versacci, Marco Tartaglia, Antonio Baldini, Bruno Marino. Expert Rev Mol Diagn 2017
17
25

The association between congenital heart disease and Down syndrome in prenatal life.
D Paladini, A Tartaglione, A Agangi, A Teodoro, F Forleo, A Borghese, P Martinelli. Ultrasound Obstet Gynecol 2000
52
25



Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.